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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77238Generated: October 29, 2026

Ethanolamine → (R/S)-2-hydroxy-N-(2-hydroxyethyl)-2-(4-(5-(3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)-1,2,4-oxadiazol-3-yl)phenyl)propanamide

https://huagongshe.com/reaction/77238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
Reactant4-MethylmorpholineHCID 7972—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantHCID 131731880HCID 131731880—
SolventDimethylformamideHCID 6228—
Product(R/S)-2-hydroxy-N-(2-hydroxyethyl)-2-(4-(5-(3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)-1,2,4-oxadiazol-3-yl)phenyl)propanamideHCID 6745835614.7%

Reaction Steps

(R/S)-2-Hydroxy-2-(4-(5-(3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)-1,2,4-oxadiazol-3-yl)phenyl)propanoic acid (Int-XV, 30 mg, 0.067 mmol), BOP (29.8 mg, 0.067 mmol), 4-methylmorpholine (27.3 mg, 0.269 mmol), and 2-aminoethanol (6.17 mg, 0.101 mmol) were added to DMF (1 mL). The reaction mixture was stirred for 1 h and then purified by prep HPLC (PHENOMENEX® 21×250 mm, gradient elution with Method 1—MeOH/water containing 0.1% trifluoroacetic acid as defined above, 0% B to 100% B over 30 min, 25 mL/min, 220 nM, product retention=30.0 min) to provide (R/S)-2-hydroxy-N-(2-hydroxyethyl)-2-(4-(5-(3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)-1,2,4-oxadiazol-3-yl)phenyl)propanamide (6 mg, 9.83 μmol, 14.59% yield): LCMS=489.0 [M+H]+; 1H NMR (400 MHz, methanol-d4) δ ppm 8.10-8.21 (2 H, m), 7.53-7.92 (7 H, m), 3.60 (2 H, td, J=5.61, 3.74 Hz), 3.33-3.43 (2 H, m), 1.80 (3 H, s); HPLC peak RT=9.0 min (Method A).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835470B2
Source datasetuspto-grants-2014_09
ORD IDord-58e0dd949a774796b84b734a0374d81b
Source noteuspto-grants-2014_09